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Updated: Jan 31, 2026

In Vivo Imaging and Quantitation of the Host Angiogenic Response in Zebrafish Tumor Xenografts
Published on: August 14, 2019
Response-to-repeatability of quantitative imaging features for longitudinal response assessment
Christie Lin1, Stephanie Harmon1, Tyler Bradshaw2
1Department of Medical Physics, University of Wisconsin, Madison, WI, United States of America.
Quantitative imaging biomarkers (QIBs) require a new metric, response-to-repeatability ratio (R/R), to assess treatment response sensitivity. R/R evaluates how well QIBs detect tumor changes relative to measurement consistency, aiding biomarker selection.
Area of Science:
- Medical Imaging
- Radiomics
- Oncology
Background:
- Quantitative imaging biomarkers (QIBs) are crucial for treatment response assessment.
- Repeatability is a common metric for selecting QIBs, but sensitivity to change is also vital.
- Existing metrics do not fully capture a QIB's utility in measuring treatment effects.
Purpose of the Study:
- Introduce the response-to-repeatability ratio (R/R) to evaluate QIB sensitivity to treatment-induced changes.
- Apply R/R to PET texture features in bone-metastatic prostate cancer.
- Compare R/R with traditional repeatability metrics like ICC and CV.
Main Methods:
- Calculated R/R as the proportion of follow-up changes outside the 95% limits of agreement (LOA) derived from test-retest data.
- Analyzed 47 texture features from 18F-NaF PET/CT scans in prostate cancer patients.
- Assessed intraclass correlation coefficient (ICC) and coefficient of variation (CV) for each feature.
- Correlated R/R with ICC and CV using Spearman's rank correlation.
Main Results:
- R/R varied significantly across texture features, with 87% showing R/R > 5% and 23% showing R/R > 20%.
- Repeatability metrics (ICC, CV) showed weak correlations with R/R (ρ=0.40 and ρ=0.23, respectively), indicating limited ability to predict sensitivity to change.
- Skewness, kurtosis, and diagonal moment demonstrated high ICC (>0.75) and superior R/R values compared to SUVmax.
Conclusions:
- The R/R metric effectively characterizes the sensitivity of QIBs to detect measurable changes during treatment.
- R/R complements existing precision metrics (CV, ICC, LOA) for assessing QIB utility in treatment response evaluation.
- This approach aids in selecting robust QIBs that are both repeatable and sensitive to therapeutic effects.
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